Macrophage migration inhibitory factor (MIF) promoter polymorphism in inflammatory disease

ABSTRACT

Describe herein is a CATT-tetranucleotide repeat polymorphism at position −817 of the human Mif gene that functionally affects the activity of the Macrophage Inhibitory Factor (MIF) promoter in gene reporter assays. Four genotypes are described which comprise 5, 6, 7, or 8-CATT repeat units. Of these, the 5-CATT allele has the lowest level of basal and stimulated MIF promoter activity in vitro. The presence of the low expressing, 5-CATT repeat allele correlated with low disease severity in a cohort of rheumatoid arthritis patients. Methods, compositions and apparatus for detecting this CATT-tetranucleotide repeat polymorphism at position −817 of the human Mif gene, and for using same for assessing predisposition to severe inflammatory disease, are also disclosed.

This application claims priority from U.S. Provisional Application Ser. No. 60/341,832 filed Dec. 21, 2001. The entirety of that provisional application is incorporated herein by reference.

BACKGROUND OF THE INVENTION

1. Field of the Invention

This invention relates to diagnostic method and apparatus based upon a functional polymorphism in the promoter of a gene encoding macrophage migration inhibitory factor (MIF). More specifically, this invention relates to a method for diagnosis of pre-disposition to certain disease states, by screening for the presence of this promoter polymorphism. The invention also relates to apparatus for screening for the polymorphism, MIF genes containing the polymorphism and to a probe therefor.

2. Background of the Technology

A number of experimental studies have led to the concept that macrophage migration inhibitory factor (MIF) functions as a physiological counter-regulator of glucocorticoid action within the immune system. In this role, MIF's position within the cytokine cascade is to act in concert with endogenous glucocorticoids to control the set point and the magnitude of the inflammatory response (1). MIF also has several direct, pro-inflammatory roles in inflammatory diseases such as rheumatoid arthritis (2), sepsis (3, 4), acute respiratory distress syndrome (5), and glomerulonephritis (6).

MIF was originally described over 30 years ago as a T-lymphocyte-derived factor that inhibited the migration of peritoneal macrophages (7), but it is now known that several other cell types, including macrophages themselves, are important sources of MIF (8). MIF levels are elevated in the serum and synovial fluid of patients with rheumatoid arthritis (2, 9), and within the synovial joint MIF immunostaining can be localized to the synovial lining CD 14+ macrophages and fibroblast-like synoviocytes (2). Upon release MIF is directly pro-inflammatory by activating or promoting cytokine expression (TNFα (8, 10), IL-1β, IL-2 (11), IL-6 (8,12), IL-8 (13) and IFNγ (11, 14)), nitric oxide release (15), matrix metalloproteinase (MMP) expression (16, 17), and induction of the cyclooxygenase-2 (Cox-2) pathway (18). MIF's capacity to induce to sustained activation of the p44/p42 (ERK-1/2) MAP kinase pathway (18) and to inhibit p53-dependent apoptosis (19, 20) also suggest that this mediator may play a key role in initiation of rheumatoid pannus.

U.S. Pat. No. 6,030,615 to Bucala, et al. discloses a combination method for treating diseases caused by cytokine-mediated toxicity, comprising administering an effective amount of (a) an MIF inhibitor, such as an antibody that binds to an MIF polypeptide, wherein the MIF polypeptide has a molecular weight of about 12.5 kDa in combination with (b) anti-TNFα, anti-IL1, anti-IFN-γ, IL-1RA, a steroid, a glucocorticoid, or IL-10.

The concept that polymorphisms in immune response genes contribute to the pathogenesis of certain human autoimmune/inflammatory diseases has received increasing interest over the last several years. At present, very few gene polymorphisms have been shown to be functionally significant and to be of prognostic value in specific disease states. Previously defined examples include polymorphisms in TNFα and IL-1ra that have been shown to have certain prognostic significance in malaria and ischaemic heart disease respectively (24,25). Similarly, a number, of polymorphisms in TNFα and IL-β have been reported to be associated with rheumatoid arthritis severity (26–28).

SUMMARY OF THE INVENTION

The present invention is based in part upon identification of a novel polymorphism in the human Mif gene that consists of a tetra-nucleotide CATT repeat located at position −817 of the Mif promoter. As disclosed herein, this promoter polymorphism is functionally significant in vitro, and analysis of a cohort of patients with rheumatoid arthritis indicates that this CATT repeat is associated with disease severity.

One object of this invention, therefore, is to provide a method of diagnosis comprising determining the genotype of a human Mif promoter.

Another object of this invention is to provide diagnostic means, comprising a means for determining the genotype of a human Mif promoter.

Accordingly, the invention relates to a method of diagnosis of severity of a non-infectious inflammatory disease or of a predisposition to severity of a non-infectious inflammatory disease comprising detecting a polymorphism in a human Mif promoter that correlates with an increase or decrease in MIF polypeptide expression. In this method the non-infectious inflammatory disease is, for instance, autoimmunity, graft versus host disease, or preferably rheumatoid arthritis, and preferably detection of the polymorphism is indicative of the severity of the disease or predisposition to severity of the disease. Preferably, this polymorphism in a human Mif promoter that correlates with an increase or decrease in MIF polypeptide expression is a CATT-tretranucleotide repeat polymorphism at position −817 of the human Mif gene, selected from the group consisting of 5, 6, 7 and 8 repeat units, where presence of the 5 repeat unit indicates occurrence of or predisposition to low disease severity.

The diagnostic method of of the invention preferably comprises a step of amplifying the Mif promoter using a PCR technique. For this purpose, the invention provides a PCR primer set selected to amplify a region of a human Mif promoter. For instance, the PCR primer set may be selected from the group consisting of: (i) MIF-F (−1024) and MIF-R (−421); (ii) MIF-F (−441) and MIF-R (+4); (iii) MIF-F (−13) and MIF-R (+395); and (iv) MIF-F (+379) and MIF-R (+1043), as shown in Table 1, infra. The invention also relates to a method of using a primer set of the invention to detect a polymorphism in a human Mif promoter region, and an article of manufacture (such as a diagnostic kit) comprising a PCR primer set of the invention.

The invention further relates to nucleic acid molecule comprising a human Mif promoter sequence in which the CATT-tetranucleotide at position −817 is repeated 5, 6, 7 or 8 times. Preferably, the nucleic acid molecule is an isolated DNA molecule, particularly an isolated genomic DNA fragment that has been amplified from a DNA sample of a human subject. In preferred embodiments, the isolated nucleic acid molecule of the invention comprises a portion of a human Mif promoter that comprises a CATT-tretranucleotide repeat polymorphism at position −817 of the human Mif gene.

Another aspect of the present invention relates to a method of inflammatory disease therapy comprising screening an individual for severity of a non-infectious inflammatory disease or of a predisposition to severity of a non-infectious inflammatory disease. This method comprises: detecting in a human subject a polymorphism in a human Mif promoter that correlates with an increase or decrease in MIF polypeptide expression, where detection of the polymorphism is indicative of the severity of the disease or predisposition to severity of the disease. This method of inflammatory disease therapy further comprises treating the human subject to prevent or reduce the severity of the inflammatory disease or to delay the onset of the inflammatory disease. For instance, the therapy may comprise treating the human subject by administering an effective amount of at least one agent selected from the group consisting of an MIF inhibitor, an anti-TNFα antibody, an anti-IL1 antibody, and anti-IFN-γ antibody, IL-1RA, a steroid, a glucocorticoid, and IL-10.

In a preferred embodiment of the invention method of inflammatory disease therapy the inflammatory disease is rheumatoid arthritis and the polymorphism in a human Mif promoter is a CATT-tretranucleotide repeat polymorphism at position −817 of the human Mif gene.

BRIEF DESCRIPTION OF THE FIGURES

FIG. 1 shows a schematic representation of the human Mif promoter region. Putative transcription factor binding sites and areas of interest are boxed. The polymorphic CATT repeat region (−817 to −797/−785) is indicated by a lack of shading.

FIG. 2 shows the basal transcriptional activity of human Mif promoter polymorphic variants in Cos-7 cells. MIF promoter activity was determined by dual luciferase assays with results expressed as relative light units (RLU). Cos-7 cells were transiently co-transfected with 800 ng of test DNA vector: pGL3-basic (negative control), pMIF-5, pMIF-6, pMIF-7, or pMIF-8 (5, 6, 7, or 8-CATT repeat polymorphism specific MIF promoter-luciferase constructs) and 200 ng of control pRLTK vector. After 48 hours, the cells were lysed and luciferase activity was determined in relation to renilla activity using a dual luciferase kit (Promega) and a TD 20/20 luminometer. The data represent the mean of four individual experiments each carried out in duplicate ±STDEV. * indicates P<0.03 vs. activity of pMIF-5 construct.

FIG. 3 shows the effect of CATT-repeat polymorphic variation on Mif promoter responses to serum and forskolin stimulation in Cos-7 cells. MIF promoter activity was determined by dual luciferase assays with results expressed as relative light units (RLU). Cos-7 cells were transiently co-transfected with 800 ng of test DNA vector: pGL3-basic (negative control), pMIF-5, pMIF-6, pMIF-7, or pMIF-8 (5, 6, 7, or 8-CATT repeat polymorphism specific MIF promoter—luciferase constructs) and 200 ng of control pRLTK vector. After 24 hours of transfection, the cells were washed in PBS and then cultured in serum free media overnight. The cells were then either left unstimulated (serum starved) or treated with 2% fetal calf serum (FCS) or 1 μM forskolin (“1 uM FSK”). After a further twelve hour incubation luciferase activity was determined as in FIG. 2. The data represent the mean of four individual experiments each carried out in duplicate ±STDEV. * indicates P<0.03 vs. activity of pMIF-5 construct.

FIGS. 4A and 4B depicts the nucleic acid sequence for human Mif (SEQ ID NO: 12). The nucleotide position designated as −817 in the figure is position 259 of SEQ ID NO: 12.

DETAILED DESCRIPTION OF THE INVENTION

The novel Mif gene polymorphism identified herein is associated with reduced MIF promoter activity, and the presence of this genotype in the homozygous state appears to be associated with a reduced risk of severe rheumatoid arthritis.

MIF has been shown to promote TNFα secretion and to enhance IFNγ induced nitric oxide secretion from macrophages (8). In addition, MIF is an important autocrine regulator of macrophage (8), T-cell (11) and fibroblast activation (18). These data have led to numerous investigations of the potential role for MIF in chronic inflammatory conditions such as rheumatoid arthritis.

MIF protein levels circulate in higher levels in serum of rheumatoid arthritis patients and cellular MIF expression is enhanced within the synovium (2, 9). Cultured synovial fibroblasts obtained from patients with rheumatoid arthritis secrete significant quantities of MIF spontaneously in culture, and secretion increases further following pro-inflammatory stimulation (2). MIF stimulation of rheumatoid synovial fibroblasts results in increased expression of matrix metalloproteinases (16), as well as the induction of phospholipase A₂ (PLA₂) and COX-2 expression (29). Immunoneutralization of MIF activity in synoviocyte cultures also has been shown to inhibit IL-Iβ induced expression of COX-2 and PLA₂ mRNA (29). The administration of a neutralizing anti-MIF antibody also delays the onset and decreases the severity of type-II collagen induced arthritis in mice (30) and profoundly inhibits the development of adjuvant-induced arthritis in rats (31). Thus, there is considerable evidence implicating MIF in the pathogenesis of inflammatory arthritis.

Disclosed herein is a significant association between patients that are homozygous for the low expressing, 5-CATT allele and less aggressive rheumatoid disease. Only 1/79 (1.2%) patients with severe rheumatoid arthritis inherited this genotype, compared with 101105 (9.5%) of patients with milder, non-progressive disease. This suggests that a genetic predisposition to low expression of MIF protects against persistent inflammation and/or joint destruction. It is unknown at present which transcription factors may be involved in modulating the transcriptional effects of the polymorphic region, but the 5-CATT allele shows reduced responses in vitro to both serum and forskolin stimulation as well as reduced basal activity. A CATT repeated element also exists in the promoter of human granulocyte-macrophage colony-stimulating factor (GM-CSF), and is required for promoter activity (32, 33). It has been shown that the nuclear factor YY1³⁴, and more recently the factors AP-1 and SP-1, can form complexes with this region of the GM-CSF promoter (35). Whether any of these same factors also influence the activity of the MIF CATT repeat remains to be determined.

The CATT-repeat region within the Mif gene contains several putative Pit-1 transcription factor binding sites. Pit-1 is a pituitary-specific transcription factor that is critical for the expression of pituitary hormones such as prolactin and growth hormone (36). The anterior pituitary gland is an important source of MIF in rodents (3) and secretes MIF in response to physiological or infective stress (37). Corticotrophin-releasing factor (CRF) also has been shown to be a potent inducer of MIF expression in cultured pituitary cells. A recent functional analysis of the murine MIF gene-promoter using rat pituitary cells and the pituitary cell line AtT-20 demonstrated that CRF-induced gene expression is dependent upon a cAMP responsive element binding protein (38). Interestingly, reports of linkage of the CRF locus to rheumatoid arthritis have recently appeared in the literature, and there is some evidence that the hypothalamic pituitary—adrenal (HPA) axis may play a role in the pathogenesis of rheumatoid arthritis in certain patients. Patients with active rheumatoid arthritis have been shown to have abnormally low diurnal cortisol levels in the face of normal pituitary and adrenal function, suggesting a defect at the hypothalamic level (40). Given MIF's capacity to counter-regulate glucocorticoid action within the immune system (reviewed by Bucala (1)), the expression of MIF by the anterior pituitary gland may be important to the development of inflammatory diseases such as rheumatoid arthritis.

Since the initiation of these studies, a −173*G/C single nucleotide polymorphism (SNP) in the Mif gene promoter has been reported by Donn, et al. (41) and was shown to be associated with systemic-onset juvenile idiopathic arthritis (systemic-onset JIA). The possession of at least one 173*C allele was seen in 36.8% of patients with systemic-onset JIA compared to 20.3% of the normal population (41). However, there is no information concerning the effect of this SNP on gene expression. A preliminary analysis by the present inventors indicates that the 173*C allele cannot explain the present association data or results of promoter assays; indeed, there is no evidence of positive linkage disequilibrium between the 173*C allele and the 5-CAAT allele (data not shown).

TNFα is considered to be a critical effector cytokine in rheumatoid arthritis, and anti-TNFα therapy has emerged to have high efficacy in the treatment of this disease (42). Of note, there is a close relationship between MIF and TNFα. MIF appears to act as an important upstream regulator of TNFα expression. MIF promotes secretion of TNFα from macrophages and overrides the ability of glucocorticoids to suppress macrophage TNFα production (43). Immunoneutralization of MIF also reduces circulating levels of TNFα (3). In a clinical setting, the analysis of MIF polymorphisms provides a prognosticator of disease severity, particularly in inflammatory diseases and more particularly in rheumatoid disease, and can assist in the selection of interventional therapy. The data herein also reaffirm the potential importance of MIF as a therapeutic target in rheumatoid arthritis and possibly other inflammatory diseases.

Experimental Materials and Methods

Patients: DNA samples were obtained from the Wichita Rheumatic Disease Data Bank and were representative of Caucasian patients followed in a rheumatology practice since 1974. The rheumatoid arthritis patients were divided into 2 groups using the following criteria: A) Severe (n=79); mean age at onset 55 years, mean disease duration of 13 years, mean Larsen score rate of 4.0, mean RF titer of 339.24 and a mean HAQ score.o.f 1.36. B) Mild (n=105); mean age at onset 45 years, mean disease duration of 15 years, mean Larsen score of 1.0, mean RF titer of 362.84 and a mean HAQ score of 0.93. Healthy Caucasian volunteers provided genomic DNA that was used as the normal control group (n=159).

DNA extraction: DNA was extracted from whole blood using the G Nome kit (Bio 101 Inc., CA, USA) and from the buccal brushes using the Pure Gene Kit® (Gentra Systems Inc., MN, USA).

Mif gene Sequencing and Polymorphism analysis: The Mif gene (GenBank Accession number: L19686, hereby incorporated in its entirety herein by reference) is located on chromosome 22q11.2 (44). The gene is 2167 bp long and has 3 exons separated by 2 introns of 189 bp and 95 bp. Four sets of primers were used to span the entire gene (Table 1, below).

TABLE 1 Primer sequences and conditions for PCR of the Mif Gene Annealing PCR PCR Primer Primer Sequences Temp Special Product Set Locations (5′-3′) (° C.) Conditions Size SET MIF-F (−1074) TGCAGGAACCAATACCCATAGG (SEQ. ID NO:1) 58.1 654 bp 1 MIF-R (−421) TGCGTGAGCTTGTGTGTTTGAG (SEQ. ID NO:2) SET MIF-F (−441) TCAAACACACAAGCTCACGCA (SEQ. ID NO:3) 60.8 10% DMSO 445 bp 2 MIF-R (+4) TGGTCCCGCCTTTTGTG (SEQ. ID NO:4) SET MIF-F (−13) CACAAAAGGCGGGACCACA (SEQ. ID NO:5) 62.3 25% 7-Deaza 408 bp 3 MIF-R (+395) ACTGCGAGGAAAGGGCG (SEQ. ID NO:6) GTP in 1.25 mM dNTP SET MIF-F (+379) CGCCCTTTCCTCGCAGT (SEQ. ID NO:7) 10% DMSO 665 bp 4 MIF-R (+1043) TAGAATGGAAAGACACTGGG (SEQ. ID NO:8) The PCR reaction consisted of 1×PCR buffer II (Perkin Elmer, CA, USA), 20 ng DNA, 1.5 mM MgCl₂, 20 pmoles each of forward and reverse primers and 0.5 units of Amplitaq Gold® polymerase (Perkin Elmer—Applied Biosystems, CA, USA). The dNTP were used at a concentration of 0.2 mM except for set 3, where the 0.2 mM dNTP had 0.05 mM of 7-Deaza GTP in a 20 μl PCR reaction. The PCR conditions were as follows: 95° C./12 min, followed by 40 cycles of 95° C./30 sec, annealing temp (Table 1)/30 sec, 72° C./60 sec and 72° C./10 min. The PCR products were resolved using a 1% agarose gel stained with ethidium bromide.

The PCR products from 6 normal controls and 6 rheumatoid arthritis patients were sequenced using the Big Dye Terminator® cycle sequencing ready reaction kit (Perkin Elmer-Applied Biosystems). The sequences from all four primer sets were compiled to represent the entire Mif gene and were compared to analyze differences between the rheumatoid arthritis group and the normal controls.

Rapid screening for CATT repeat polymorphism: The forward primer from Set 1 (SEQ. ID. NO: 1) was used with the reverse primer MIF-R-728 (5′-AATGGTAAACTCGGGGAC-3′; SEQ. ID NO: 9). The reverse primer was fluorescently labeled with TET to allow detection of the PCR products using capillary electrophoresis (45).

The PCR conditions were 1×PCR Buffer II, 1.5 mM MgCl₂, 0.2 mM dNTP, 0.75 pmoles of each primer, 1 ng DNA, 0.05 μl AmpliTaq Gold® polymerase in a 10 μl PCR reaction. The PCR cycling conditions used were the same as described above except for annealing conditions of 53.8° C./30 sec. 1 μl of diluted PCR product was added to 12 μl of deionized formamide containing 0.5 μl GS-500 TAMRA size standard (Perkin Elmer-Applied Biosystems). Samples were denatured before being resolved using an ABI 310 Genetic Analyzer (Perkin Elmer-Applied Biosystems). DNA samples from homozygous individuals that previously had been fully sequenced were used as controls for the repeat sizes obtained by capillary electrophoresis.

MIF Promoter cloning and Reporter Assays: Genomic DNA obtained from the primary screening that contained the 5, 6, 7, or 8-CATT tetranucleotide repeat polymorphism was used as a PCR template for initial cloning into the pCR2.1-TOPO vector (Invitrogen, CA, USA). The following primers were used to generate a 1173–1189 bp PCR product representing 1071–1087 bp of the upstream flanking region of the MIF coding sequence plus the first 102 bp of exon I (see FIG. 1):

Forward primer: 5′-CTCGAGCTGCAGGAACCAATACCCAT-3′ (SEQ. ID NO:10); Reverse primer: 5′-AAGCTTGGCATGATGGCAGAAGGACC-3′ (SEQ. ID NO:12).

After complete sequencing, the promoter region was excised from the pCR2.1 vector and cloned into the Xhol/HindIII sites of the pGL3-Basic luciferase vector (Promega, Wis., USA). This vector contains the CDNA encoding a modified version of firefly luciferase in the absence of eukaryotic enhancer or promoter elements. Luciferase constructs directly regulated by the MIF promoter, containing the 5, 6, 7, or 8-CATT polymorphism, were generated. Transient transfections were carried out using 3 μl Fugene 6 (Roche, N.J., USA) and 1 μg of DNA per well of a six well plate as per manufacturers directions. Cell lines used included Cos-7 (monkey kidney fibroblast), A549 (human lung epithelium) and CCD-19LU (primary human lung fibroblast). Data were normalized in relation to an internal control of Renilla luciferase that was regulated by the Herpes simplex virus thymidine kinase promoter (PRL-TK vector—Promega, Wis., USA). Subsequently, each transfection consisted of 800 ng of test DNA (MIF-promoter regulated Luciferase gene) combined with 200 ng of PRL-TK control vector DNA. Luciferase assays were measured using a TD-20/20 luminometer (Turner Designs, Calif., USA) and the Dual Luciferase Reporter System (Promega, Wis., USA). Basal promoter activity was determined by measuring luciferase activity 36 hours after transfection. In some cases, cells were stimulated for the last 20 hours of culture prior to measurement of promoter activity.

Genotype and statistical analysis: The data were analyzed using Genotyper® 2.1 software (Perkin Elmer—Applied Biosystems, Calif., USA). The relationship between the genotypes and disease status (normal, mild or severe) was examined using the chi-square test and Fishers' exact test. Gene reporter assays were repeated 3 to 10 times in duplicate. Data are presented as mean±STDEV and compared by non-parametric Mann-Whitney U tests. Significance was defined as P<0.05.

Results

Identification of a Microsatellite Repeat in the Mif Promoter. Genomic DNA from six normal volunteers and six rheumatoid patients was utilized for full sequencing of the Mif gene. Due to the high GC content of this gene, the analysis was carried out in four sections. Alignment of all twelve sequences identified a tetra-nucleotide CATT repeat polymorphism in the upstream promoter region at position −817 (FIG. 1). Individuals having 5, 6, 7 or 8-CATT repeat alleles in their sequences were found. Individuals were either heterozygous or homozygous for these alleles, although no 7-CATT homozygotes were found in the normal population and no 8-CATT homozygotes were found in either population studied.

For rapid screening of the promoter polymorphism, a fluorescently labeled reverse primer that was proximal to the tetranucleotide repeat units was designed in order to amplify a smaller PCR fragment (340–352 bp). This fragment then was analyzed using capillary electrophoresis on an ABI 310 Genetic analyzer. The DNA of individuals previously sequenced was used as a template to generate control DNA fragments in order to correlate the fragment size observed on the ABI 310 analyzer with the number of CATT repeats in the test samples. Accordingly, the 4 PCR product sizes were 340, 344, 348, and 352 bp in length, and these corresponded to five, six, seven, and eight-CATT repeats, respectively. The genotypes observed were: 5,5; 5,6; 5,7; 6,6; 6,7; 7,7; 5,8; and 6,8. The 8,8 genotype was not seen in either the normal (n=159) or patient (n=184) populations; and the 7,7 genotype was not seen in the normal population, but was observed in one patient within the rheumatoid arthritis group.

Distribution of Mif Alleles in Normal Controls and Rheumatoid Arthritis Patients. The distribution of the different Mif alleles in normal controls, mild rheumatoid arthritis and severe rheumatoid arthritis patients are shown in Table 2, below.

TABLE 2 Distribution of MIF genotypes and the frequency of 5-CATT allele in normal and rheumatoid arthritis (RA) popluations. Frequency of MIF-Genotype 5-CATT allele 5,5 or 5,X X,X Population 5,5 6,6 7,7 5,6 5,7 6,7 5,8 6,8 alleles alleles Normal  8 53  0 61 10 25  1  1 80 79 (n = 159) (5.03%) (33.33%) (38.36%) (6.3%) (15.72%) (0.63%) (0.63%) (50.31%) (49.69%) Wichita 10 49  1 23  8 14  0  0 41 64 Mild RA (9.52%) (46.67%) (0.95%) (21.91%) (7.62%) (13.33%) (39.05%) (60.95%) (n = 105) Wichita  1 40  0 20  4 13  0  1 25 54 Severe RA (1.27%) (50.63%) (25.31%) (5.06%) (16.46%) (1.27%) (31.65%) (68.35%) (n = 79) There was no deviation from Hardy-Weinberg equilibrium in normal controls (p=0.69). The frequencies of the 5, 6, 7 and 8 alleles were found to be 0.277, 0.607, 0.11 and 0.006 respectively.

The number of individuals carrying at least one 5-CATT allele decreases from 50.31% in the normal population to 31.65% in the severe rheumatoid arthritis population (Table 2). The difference between the severe rheumatoid arthritis patients and controls is statistically significant (p<0.02). The cases and controls analyzed in this study were not closely matched for geographic and ethnic origin, hence the data must be interpreted with some caution. A comparison of specific genotypes between the mild and severe rheumatoid arthritis populations was therefore carried out, as shown in Table 2. The 5,5 genotype is observed in 9.5% of the patients with mild rheumatoid arthritis, but is significantly decreased to 1.3% in the patients with severe disease (p=0.0252 by Fisher's exact test). These data indicate that a homozygous 5-CATT allele is protective for the development of severe disease.

Effect of the CATT repeat polymorphism on MIF promoter activity. To investigate whether the CATT repeat polymorphism was associated with functional regulation of MIF expression, a gene reporter assay was developed and studied under defined conditions in vitro. Gene reporter assays have been widely employed to study transcriptional regulation, or as readouts to monitor transcription factor (21,22).

Transfection of the Mif promoter-regulated luciferase constructs into Cos-7 cells, A549 cells, and CCD-19Lu cells was associated with strong basal promoter activity, as indicated by high luciferase production, when compared to control vector (pGL3-Basic) (FIG. 2 and data not shown). Promoter activity was increased by forskolin (an inducer of CAMP synthesis 23) and serum stimulation (FIG. 3), as well as phorbol ester stimulation (data not shown). In general, basal promoter activity was high in each of the cell lines tested when compared to negative (empty pGL3 vector) and positive (pRL-TK) controls, and these data appeared to correlate with the high level of endogenous MIF protein expression that was observed in these cell lines (data not shown). Of note, in each of the cell lines tested, the 5-CATT repeat MIF promoter construct showed significantly lower transcriptional activity when compared to the 6, 7, or 8-CATT repeat promoter constructs.

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All patents, patent applications and publications mentioned hereinabove are hereby incorporated by reference in their entirety.

While the foregoing invention has been described in some detail for purposes of clarity and understanding, it will be appreciated by one skilled in the art from a reading of this disclosure that various changes in form and detail can be made without departing from the true scope of the invention and appended claims. 

1. A method of detecting a CATT tetranucleotide repeat polymorphism in the promoter of the human macrophage inhibitory factor gene, SEQ ID NO: 12, wherein the CATT tetranucleotide repeat begins at position 259 of SEQ ID NO: 12, comprising: amplifying the promoter with a PCR primer set, analyzing the size of the amplified product to determine how many CATT tetranucleotide repeats are present, and detecting 5, 7 or 8 CATT tetranucleotide repeats.
 2. The method of claim 1 wherein said PCR primer set is SEQ ID NO: 1 and SEQ ID NO:
 2. 3. The method of claim 1 wherein said PCR primer set is SEQ ID NO: 1 and SEQ ID NO:
 9. 